Our experimental systems include rodent brain slices, primary neuronal cultures, and reprogrammed human neurons
We perform knockout, knockdown, overexpression, and mutagenesis of neuronal genes to study their cellular function
A primary hippocampal neuron loaded with fluorescent dye (Alexa-594), and imaged using a laser confocal microscope
Actively recycling presynaptic terminals (arrowsheads) are labeled with FM 1-43 probe, and monitored for vesicle release
This neuron is infected with a lentivirus expressing EGFP (green) and an epitope-tagged postsynaptic protein (red)
An autism-associated mutation (blue residue, top) causes glycosylation defects (western blot, below) in a synaptic protein
The cell is patched with an electrode and its functional properties are recorded using voltage/current clamp
Single cell qPCR indicates high (red) or low (blue) expression of different genes (columns) in individual neurons (rows)